Intramolecular excimer formation by phthaloyl, isophthaloyl and terephthaloyl groups in polyesters with different numbers of methylene and oxyethylene spacers
Author:
Publisher
Elsevier BV
Subject
Polymers and Plastics,Materials Chemistry,Organic Chemistry
Reference10 articles.
1. Dependence of the occupancy of excimer-forming conformations on the size of the flexible spacer in polyesters from terephthalic acid and mono-, di- or triethylene glycol
2. Identification of conformations conducive to intramolecular excimer formation in polyesters with different numbers of methylene units between aromatic rings
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1. Thermodynamics of Complexation of Dimethyl Esters of Tere-, Iso-, and Phthalic Acids with α- and β-Cyclodextrins;Applied Spectroscopy;2004-07
2. Intramolecular excited state complexes in trichromophoric model compounds for polyesters derived from 2,6-naphthalenedicarboxylic acid and aliphatic glycols: experiment, rotational isomeric state model, and molecular dynamics;Journal of Polymer Science Part B: Polymer Physics;1999-02-01
3. Intramolecular formation of excimers in model compounds for polymers of 2,6-naphthalene dicarboxylic acid and five glycols in media of different viscosity;Journal of Polymer Science Part B: Polymer Physics;1996-11-15
4. Rationalization of the ratio of excimer-to-monomer fluorescence emission intensity in bichromophoric diesters of 1-pyrenoic acid and mono-, di-, tri-, and tetraethylene glycols;Journal of Polymer Science Part B: Polymer Physics;1995-05
5. Photophysical models of aromatic polyesters: excited state interactions in bis(phenalkyl)terephthalate;Polymer Bulletin;1995-03
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